Variant #0000515111 (NC_000002.11:g.233414160A>G, NM_005199.4:c.*3734A>G (CHRNG))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.233414160A>G
DNA change (hg38) g.232549450A>G
Published as TIGD1(NM_145702.1):c.433T>C (p.(Phe145Leu))
ISCN -
DB-ID CHRNG_000080
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EIF4E2 NM_004846.2 -?/. - c.-1275A>G r.(?) p.(=)
CHRNG NM_005199.4 -?/. - c.*3734A>G r.(=) p.(=)
TIGD1 NM_145702.1 -?/. - c.433T>C r.(?) p.(Phe145Leu)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.